PUMA System

FDA 510(k) K171703 · Panther Orthopedics, Inc.

Substantially Equivalent

510(k) numberK171703

Submission

Device name
PUMA System
Applicant
Panther Orthopedics, Inc.
San Jose, CA, US
Received
June 8, 2017
Decision date
March 1, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HTN – Washer, Bolt Nut
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3030
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was PUMA System cleared by the FDA?

PUMA System (K171703) received a 510(k) decision of Substantially Equivalent on March 1, 2018, 266 days after the submission was received.

What is the product code of K171703?

The FDA product code is HTN – Washer, Bolt Nut, a Class II (moderate risk) device regulated under 21 CFR 888.3030.